Inheritance And Selection Flashcards

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1
Q

🔴️Stabilising selection

A
  1. occurs when the environment favours those with the most common (mean) characteristic
  2. those on the extreme dies out
  3. the frequency of the common characteristic increases
  4. the range of characteristic (standard deviation) will reduce
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2
Q

🔴️Despite being 25% likely to inherit a ff allele, why doesn’t this happen?

A

1 Random fusion of gametes

2 Small sample

3 Gametes not produced in equal numbers

4 Offspring ratios are probabilities not fixed

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3
Q

Recessive allele

A

Only expressed in phenotype if homozygous;

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4
Q

Co-dominant allele

A

If both present, then both are expressed in phenotype

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5
Q

Why are genetic disease more prevalent in small, isolated populations?

A

1 Reproductively isolated so there is a small gene pool.

2 Inbreeding may occur so there is a high probability of mating with person having recessive allele

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6
Q

Why is the actual popluation without the disease higher than predicted by the H-W calculation

A

1 People with the disease may die young so they may not reach reproductive age (adult)

2 There is a selective disadvantage

3 Genetic screening helps prevent genetic diesease being perpetuated.

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7
Q

Describe and explain speciation

A

1 geographical isolation of organism;

2 Separate gene pool as no interbreeding between organisms

3 Different environmental conditions in each place

4 This means there are different selection pressures in separate populations;

4 Variation in population due to chance mutation occurs, causing organisms to acquire advanatageous allele

5 This advantageous phenotype makes indivudials more suited to their environment, and so more likely to survive and repoduce

6 The beneficial allele more likely to be passed on, increasing the frequency of the allele;

7 Over a long time, the populations have changed so much that they’re unable to produce fertile offspring

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8
Q

Explain why Males are more likely to show a phenotype produced by a recessive allele carried on the X chromosome.

A

1 Males have one allele** for each gene so recessive alleles **always expressed in Male;

2 Females need two recessive allele (homozygous recessive)

3 females recessive alleles can be masked by dominant allele

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9
Q

Explain Phenotype

A
  • Expression of a characteristic
  • due to genotype and environment;
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10
Q

Dominant allele

A

characteristic Is always expressed in the phenotype when present

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11
Q

What is a sex-linked gene?

A

a gene carried on one of the sex chromosomes, normally the X chromosome

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12
Q

Directional selection

A
  • When the environment favours those with a feature/allele as it confers advantage
  • so more likely to survive and reproduce;
  • The allelic frequencies increases so more individuals with feature
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13
Q

Species

A
  • group of organisms with similar physiological features;
  • which can interbreed to produce fertile offspring;
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14
Q

An allele may be present in the genotype but its effects are not seen in the phenotype. In terms of protein production, explain why

A
  • Effect of recessive allele not seen when dominant allele present

This is true if the:

  • Recessive allele codes for non-functional protein;
  • Dominant allele codes for functional protein;
  • Therefore the effect nullifies the recessive
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15
Q

Homologous chromosomes

A
  • Capable of pairing during meiosis
  • Same gene loci;
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16
Q

What’s the H-W principle

A
  • The proportion of alleles** of a particular **gene
  • Will stay constant from one generation to the next
  • Providing no mutation, mating at random and no migration;
17
Q

How do you know a disease is caused by a recessive allele?

A
  • 2 unaffected parents (X,Y) give birth to (Z) affected
  • Parents must both be heterozygous
18
Q

How do you know if a disease is caused by a gene on the X chromosome

A
  • Uaffected fathers (XY) give birth to affected sons
  • Mother gives the X chromosome to son and father gives the Y
19
Q

Explain how mutation may produce multiple alleles of a gene.

A
  • Changes base sequence
  • In different places within gene;